Chronic Kidney Disease Clinical Trial
— CREAM 1Official title:
Circadian Rhythm of Erythropoietin and Melatonin in Patients With Various Degrees of Renal Insufficiency
Verified date | June 2008 |
Source | Meander Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | Netherlands: Medical Ethics Review Committee (METC) |
Study type | Observational |
Rationale: Investigation of the circadian rhythm of erythropoietin and melatonin in patients
with various degrees of renal insufficiency
Objectives:
Primary objective: Is there a circadian rhythm of epo and melatonin in patients with various
degrees of renal insufficiency?
Primary Objective: Is there a circadian rhythm of epo and melatonin in patients with various
degrees of renal insufficiency compared to patients with a normal renal function?
Secondary Objective: Is there a circadian rhythm of cortisol and IGF in patients with
various degrees of renal insufficiency?
Secondary Objective: Is there a circadian rhythm of cortisol and IGF in patients with
various degrees of renal insufficiency compared to patients with a normal renal function?
Study design: Comparative study in 4 groups with various degrees of renal insufficiency,
duration for each patient 24 hrs. Total duration of study 12 months, patients admitted to
the hospital (on nursing ward)
Study population: Patients with various degrees of renal insufficiency
Main study parameters/endpoints: Analysis of the existence of a circadian rhythm in patients
with a normal renal function and in patients with variable degrees of renal insufficiency
Nature and extent of the burden and risks associated with participation, benefit and group
relatedness: Better knowledge of the circadian rhythm in renal insufficiency. This could
lead to a more efficient administration of erythropoietin and melatonin in the future.
Extent of burden is 1 venapunction for placement of infusion needle, the withdrawal of 11
times 5 ml blood in 24 hrs, continuous measurement of body temperature via capsule, 24-hour
continuous ambulant blood pressure monitoring.
Status | Completed |
Enrollment | 34 |
Est. completion date | June 2008 |
Est. primary completion date | June 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion criteria: - Patient with various degrees of renal insufficiency, stable creatinin clearance: minimum 10 ml/min (measured with MDRD), admitted to our hospital - Informed Consent - Man/Women between 18 and 85 years - Understanding and knowledge of the dutch language Exclusion criteria: - Instable angina pectoris, heart failure NYHA class IV - Therapy with erythropoetin, melatonin and hypnotics - Acute renal failure or rapidly progressive glomerulonephritis - Bleeding or hemolysis as a cause of anemia - Deficiency of iron, folate and/or vitamin B12 - Presence of chronic inflammatory disease or clinically significant infection - Hemoglobinopathies - Alcohol and/or drug abuse - Enrolment in another study - Any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Netherlands | Meander Medical Center | Amersfoort |
Lead Sponsor | Collaborator |
---|---|
Meander Medical Center | Hoffmann-La Roche, Stichting Bijstand, Meander Medical Center |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | existence of circadian rhythm of Erythropoietin and Melatonin | 24 hours | No | |
Secondary | existence of a circadian rhythm of cortisol and IGF-1 | 24 hours | No | |
Secondary | Relationship between temperature and melatonin. Relationship between blood pressure and erythropoietin | 24 hours | No |
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